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DO Term : immunoglobulin alpha deficiency [DOID:0060025] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor.

synonyms:
UMLS_CUI:C0162538,
OMIM:137100,
OMIM:609529,
609529,
GARD:10197,
MESH:D017098,
269650,
137100,
SNOMEDCT_US_2023_03_01:29260007,
gamma-A-globulin deficiency,
ORDO:69127,
IgA deficiency,
OMIM:269650

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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